Crystal structure of complex between nuclear coactivator binding domain of CBP and [1040-1086]ACTR containing alpha-methylated Leu1055 and Leu1076. Determined by X-ray diffraction at 2.28 Å resolution. Released 30 Sept 2020.
Explore 6SQC in 3D Show helices and sheets RCSB PDB PDBe
6SQC contains 32 α-helices and 24 β-strands across 2 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 1690-1692 | 3 | |
| β-strand | 1696-1699 | 4 | 1 |
| α-helix | 1706-1720 | 15 | |
| β-strand | 1724-1727 | 4 | 1 |
| α-helix | 1732-1739 | 8 | |
| α-helix | 1740-1742 | 3 | |
| β-strand | 1748-1752 | 5 | 1 |
| α-helix | 1753-1755 | 3 | |
| α-helix | 1756-1761 | 6 | |
| β-strand | 1765 | 1 | 2 |
| α-helix | 1766-1767 | 2 | |
| β-strand | 1768 | 1 | 3 |
| α-helix | 1772-1775 | 4 | |
| β-strand | 1778 | 1 | 4 |
| α-helix | 1780-1785 | 6 | |
| β-strand | 1787-1788 | 2 | 3 |
| β-strand | 1791-1792 | 2 | 3 |
| β-strand | 1795-1800 | 6 | 1 |
| β-strand | 1803-1807 | 5 | 5 |
| β-strand | 1817 | 1 | 6 |
| α-helix | 1821-1829 | 9 | |
| β-strand | 1834-1836 | 3 | 5 |
| α-helix | 1843-1851 | 9 | |
| β-strand | 1856-1861 | 6 | 7 |
| β-strand | 1864-1871 | 8 | 7 |
| α-helix | 1875-1889 | 15 | |
| α-helix | 1899-1907 | 9 | |
| β-strand | 1911-1916 | 6 | 5 |
| α-helix | 1918-1920 | 3 | |
| α-helix | 1921-1926 | 6 | |
| β-strand | 1931-1934 | 4 | 5 |
| α-helix | 1935-1937 | 3 | |
| β-strand | 1938-1939 | 2 | 6 |
| β-strand | 1942-1943 | 2 | 6 |
| α-helix | 1944 | 1 | |
| β-strand | 1947-1948 | 2 | 8 |
| β-strand | 1949-1955 | 7 | 1 |
| β-strand | 1956 | 1 | 2 |
| α-helix | 1962-1968 | 7 | |
| α-helix | 1969-1973 | 5 | |
| α-helix | 1976-1985 | 10 | |
| β-strand | 1990-1991 | 2 | 1 |
| β-strand | 1993 | 1 | 4 |
| α-helix | 1994-1999 | 6 | |
| α-helix | 2004-2015 | 12 | |
| β-strand | 2017-2018 | 2 | 8 |
| α-helix | 2019-2020 | 2 | |
| α-helix | 2025-2040 | 16 | |
| α-helix | 2046-2055 | 10 | |
| α-helix | 2064-2065 | 2 | |
| α-helix | 2066-2074 | 9 | |
| α-helix | 2080-2092 | 13 | |
| α-helix | 2094-2110 | 17 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 1044-1058 | 15 | |
| α-helix | 1062-1070 | 9 | |
| α-helix | 1073-1080 | 8 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Maltose/maltodextrin-binding periplasmic protein,CREB-binding protein | A | protein | 424 | Escherichia coli (strain K12), Homo sapiens | P0AEX9 (AlphaFold model), Q92793 (AlphaFold model) |
| Nuclear receptor coactivator 3 | B | protein | 47 | Homo sapiens | Q9Y6Q9 (AlphaFold model) |
>6SQC_1 Maltose/maltodextrin-binding periplasmic protein,CREB-binding protein (chains A) MKIEEGKLVIWINGDKGYNGLAEVGKKFEKDTGIKVTVEHPDKLEEKFPQVAATGDGPDI IFWAHDRFGGYAQSGLLAEITPAAAFQDKLYPFTWDAVRYNGKLIAYPIAVEALSLIYNK DLLPNPPKTWEEIPALDKELKAKGKSALMFNLQEPYFTWPLIAADGGYAFKYENGKYDIK DVGVDNAGAKAGLTFLVDLIKNKHMNADTDYSIAEAAFNKGETAMTINGPWAWSNIDTSA VNYGVTVLPTFKGQPSKPFVGVLSAGINAASPNKELAKEFLENYLLTDEGLEAVNKDKPL GAVALKSYEEELAKDPRIAATMENAQKGEIMPNIPQMSAFWYAVRTAVINAASGRQTVDA ALAAAQTNAAAMSISPSALQDLLRTLKSPSSPQQQQQVLNILKSNPQLMAAFIKQRTAKY VANQ
>6SQC_2 Nuclear receptor coactivator 3 (chains B) EGQSDERALLDQLHTLLSNTDATGLEEIDRALGIPELVNQGQALEPK
| ID | Name | Formula | Copies |
|---|---|---|---|
| ZN | Zinc ion | Zn | 2 |
Water and common crystallization additives (EDO) are not listed.
Conformational editing of intrinsically disordered protein by alpha-methylation. Bauer, V., Schmidtgall, B., Gogl, G. et al. Chem Sci (2020) 12:1080-1089. DOI 10.1039/d0sc04482b · PubMed
Other PDB entries of the same protein (UniProt P0AEX9 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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